Predicting in vivo cardiovascular properties of blockers from cellular assays: a quantitative comparison of cellular and cardiovascular pharmacological responses

Date

2011-08-24

Advisors

Journal Title

Journal ISSN

ISSN

Volume Title

Publisher

FASEB

Type

Article

Peer reviewed

Yes

Abstract

Beta -Adrenoceptor antagonists differ in their degree of partial agonism. In vitro assays have provided information on ligand affinity, selectivity, and intrinsic efficacy. However, the extent to which these properties are manifest in vivo is less clear. Conscious freely moving rats, instrumented for measurement of heart rate ( 1; HR) and hindquarters vascular conductance ( 2; HVC) were used to measure receptor selectivityand ligand efficacy in vivo. CGP 20712A caused a dose-dependent decrease in basal HR (P<0.05, ANOVA) at 5 doses between 6.7 and 670 g/kg (i.v.) and shifted the dose-response curve for isoprenaline to higher agonist concentrations without altering HVC responses. In contrast, at doses of 67 g/kg (i.v.) and above, ICI 118551 substantially reduced the HVC response to isoprenaline without affecting HR responses. ZD 7114, xamoterol, and bucindolol significantly increased basal HR ( HR: 122 12, 129 11, and 59 11 beats/min, respectively; n 6), whereas other -blockers caused significant reductions (all at 2 mg/kg i.v.). The agonist effects of xamoterol and ZD 7114 were equivalent to that of the highest dose of isoprenaline. Bucindolol, however, significantly antagonized the response to the highest doses isoprenaline. An excellent correlation was obtained between in vivo and in vitro measures of 1-adrenoceptor efficacy(R2 0.93; P<0.0001).

Description

Keywords

partial agonism, intrinsic sympathomimetic, heart rate, vascular conductance

Citation

Baker, J., Kemp, P., March, J., Fretwell, L., Hill, S., and Gardiner, S. (2011) Predicting in vivo cardiovascular properties of blockers from cellular and cardiovascular pharmacological responses. The FASEB Journal. 25 (12), pp. 4486-4497

Rights

Research Institute